Canonical Allele Identifier: CA2580097005

Gene: KDM4B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5144077_5144093del , CM000681.2:g.5144077_5144093del	GRCh38
NC_000019.9:g.5144088_5144104del , CM000681.1:g.5144088_5144104del	GRCh37
NC_000019.8:g.5095088_5095104del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000159111.9:c.2661_2677del MANE Select	ENSP00000159111.3:p.Val888ArgfsTer?
ENST00000159111.8:c.2661_2677del	ENSP00000159111.3:p.Val888ArgfsTer?
ENST00000536461.5:c.2763_2779del	ENSP00000440495.1:p.Val922ArgfsTer?
ENST00000589104.5:n.2427_2443del
ENST00000611640.4:c.2763_2779del	ENSP00000480642.1:p.Val922ArgfsTer?
NM_015015.2:c.2661_2677del	NP_055830.1:p.Val888ArgfsTer?
XM_005259521.2:c.2763_2779del	XP_005259578.2:p.Val922ArgfsTer?
XM_005259522.3:c.1668_1684del	XP_005259579.2:p.Val557ArgfsTer?
XM_011527814.1:c.2487_2503del	XP_011526116.1:p.Val830ArgfsTer?
XM_011527816.1:c.1734_1750del	XP_011526118.1:p.Val579ArgfsTer?
XM_011527817.1:c.1683_1699del	XP_011526119.1:p.Val562ArgfsTer?
XM_005259521.4:c.2763_2779del	XP_005259578.2:p.Val922ArgfsTer?
XM_011527814.2:c.2487_2503del	XP_011526116.1:p.Val830ArgfsTer?
XM_011527816.2:c.1734_1750del	XP_011526118.1:p.Val579ArgfsTer?
XM_011527817.2:c.1683_1699del	XP_011526119.1:p.Val562ArgfsTer?
XM_017026503.1:c.2763_2779del	XP_016881992.1:p.Val922ArgfsTer?
NM_015015.3:c.2661_2677del MANE Select	NP_055830.1:p.Val888ArgfsTer?